High-capacity alloying-type anodes suffer poor rate capability due to their great volume expansion, while high-rate intercalation-type anodes are troubled with low theoretical capacity. Herein, a novel mechanism of alloying in the intercalative frameworks is proposed to confer both high-capacity and high-rate performances on anodes. Taking the indium-vanadium oxide (IVO) as a typical system, alloying-typed In is dispersed in the stable intercalative V O to form a solid solution. The alloying-typed In element provides high lithium storage capacity, while the robust, Li-conductive V-O frameworks effectively alleviate the volume expansion and aggregation of In. Benefiting from the above merits, the anode exhibits a high specific capacity of 1364 mA h g at 1 A g and an extraordinary cyclic performance of 814 mA h g at 10 A g after 600 cycles (124.9 mA h g after 10 000 cycles at 50 A g ). The superior electrochemical rate capability of (In,V) O solid solution anode rivals that of the reported alloying anode materials. This strategy can be extended for fabricating other alloying/intercalation hybrid anodes, such as (Sn,V)O and (Sn,Ti)O , which demonstrates the universality of confining alloying motifs in intercalative frameworks for rapid and high-capacity lithium storage.
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http://dx.doi.org/10.1002/advs.202202026 | DOI Listing |
Phys Chem Chem Phys
April 2023
Department of Biomedical Engineering, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, Uttar Pradesh, India.
The electrochemical kinetics of the electrode material plays a crucial role in the development of various energy storage devices such as batteries, supercapacitors, and hybrid supercapacitors. Battery-type hybrid supercapacitors are envisaged as excellent candidates to bridge the performance gap between supercapacitors and batteries. Due to its open pore framework structure and more structural stability, porous cerium oxalate decahydrate (Ce(CO)·10HO) is found here to be a potential energy storage material partly because of the presence of planer oxalate anions (CO).
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2022
Beijing National Laboratory for Molecular Sciences and State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P. R. China.
High-capacity alloying-type anodes suffer poor rate capability due to their great volume expansion, while high-rate intercalation-type anodes are troubled with low theoretical capacity. Herein, a novel mechanism of alloying in the intercalative frameworks is proposed to confer both high-capacity and high-rate performances on anodes. Taking the indium-vanadium oxide (IVO) as a typical system, alloying-typed In is dispersed in the stable intercalative V O to form a solid solution.
View Article and Find Full Text PDFRSC Adv
October 2021
Department of Ceramic Engineering, Indian Institute of Technology (Banaras Hindu University) Varanasi Uttar Pradesh 221005 India +91-9473720659.
To overcome the environmental challenges caused by utilization of fossil fuel based energy technologies and to utilize the full potential of renewable energy sources such as solar, wind and tidal, high power and high energy density containing large scale electrochemical energy storage devices are a matter of concern and a need of the hour. Pseudocapacitors with accessibility to multiple oxidation states for redox charge transfer can achieve a higher degree of energy storage density compared to electric double layer capacitors (EDLC) and the hybrid supercapacitor is one of the prominent electrochemical capacitors that can resolve the low energy density issues associated with EDLCs. Due to its open pore framework structure with superior structural stability and accessibility of Co redox states, porous anhydrous CoCO nanorods are envisaged here as a potential energy storage electrode in a pseudo-capacitive mode.
View Article and Find Full Text PDFDalton Trans
April 2022
Department of Ceramic Engineering, Indian Institute of Technology (IIT-BHU), Varanasi, 221005, India.
The cost-effective and abundant availability of sodium offers an opportunity for rechargeable Na-ion batteries as an ideal replacement for rechargeable Li-ion batteries. However, the larger size and strong Na-Na interaction create multidimensional phase instability and transformation problems, especially in layer-structured NaMO (Mn, Co, Fe, and Ni) that inhibit the direct transformation of rechargeable Li-ion battery technology to Na-ion batteries. However, framework structures offer superior structural stability due to the interconnection of polyanions or polyhedra forming cationic octahedra.
View Article and Find Full Text PDFJ Colloid Interface Sci
June 2022
Centre for Interdisciplinary Research, D. Y. Patil Education Society, Deemed to be University, Kolhapur 416 006, India. Electronic address:
The layer-by-layer mesoporous nanohybrids of Ni-Cr-layered double hydroxide (Ni-Cr-LDH) and polyoxotungstate nanoclusters (Ni-Cr-LDH-POW) are prepared via exfoliation reassembling strategy. The intercalative hybridization of Ni-Cr-LDH with POW nanoclusters leads to forming a layer-by-layer stacking framework with significant expansion of the interplanar spacing and surface area. The aqueous hybrid supercapacitor (AHSC) and all-solid-state hybrid supercapacitor (SSHSC) devices are fabricated using Ni-Cr-LDH-POW nanohybrid as a cathode and reduced graphene oxide (rGO) as an anode material.
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